Body aches symptoms and conditions

Daughter was sick for 6 weeks with what started as a virus . Dr.'s said virus needed to run it's course and allergies were also bad so they put her on Singulair. When she wasn't improving they said she had mono. No improvement, still mono. Still not improving, more specific test, not mono. Dr's chalked it up as she had a virus and was now just depressed from being down for so long. Well when you have mono u r told not do anything and only rest. After weeks of doing this she was depressed and weak. Then we were told that the diagnosis was wrong and we were had been trying to nurse the wrong sickness. Dr's said to send her back to school. By that time our daughter was so far gone it wasn't possible. Every time we left the house she would scream and panic. Experiencing exhaustion and not her self (She loves school & was always a very happy child) I knew there had to be something wrong with her. They sent her to the hospital lab twice and found nothing. Still trying to say she is only depressed but now being rude about by saying that we were just giving her, her way. My husband & I decided that the Dr.'s were not doing there part and trying to get to the bottom of her illness. So we began looking at what had been different in her life over this period of time (5 weeks).The only thing that had changed in her life other than her catching a virus was that she was put on Singulair. We had enough common sense to know that some people may have a reaction to some medicines that others won't. And just because not every Dr. has experienced this doesn't mean it can't happen.We read the pamphlet and all of the side effects. Even the rare ones she was experiencing. Shaking that looked like seizures, body aches, numbness in fingers and toes, extreme fatigue, loss of appetite, weight loss, irrational behavior, anxiety, paranoia, coughing, depressed, swelling of the lips, hallucinations, blurred vision,screaming every time she left the house, and complaining of constant pain. We felt like that had to be what it was. So we researched it and found on medications.com story after story of children who had gone through the same thing that she was experiencing. Dr was very rude and said she had never heard of that before and just send her back to school. So my husband ad I made the decision to take her off the med. The day before we rushed her to the hospital was her last day on the Singulair. That turning point was the seizure like shaking,hallucinations, saying that she couldn't hardly see us.That night in the ER they ran a CT Scan and found nothing. They admitted her in the pediatrics unit and we began a week that felt much like a month. They started her on an IV. They called in different Dr's...resident Dr's, pediatricians, etc. Everyone said our theory on the Singulair was possible but since they had never personally experienced a case of that they just weren't sure.When no one could figure out what was wrong they then called in a neurologist. He was very concerned and immediately started assessing her and ordering blood work and tests. She had an MRI and an EEG. All came back normal. He listened to our theory and said it was possible but to be sure he wanted to test for for everything else to make sure nothing was being missed. She had lost 5 lbs before her hospital stay and not sure how much more after that but while in the hospital when I bathed her, it was so sad to see her stomach all shrunken in. They put her on 5 different medicines while in the hospital that we were so upset and torn because then we felt like she was being drugged. They had her on an IV the whole week she was there and hooked up to monitors.She had a couple of really bad episodes while she was there where she felt like she couldn't breath, couldn't stop shaking and then she lost her speech which scared us to death. They ended up sedating her to calm her down. That one episode was on a Wednesday and then Thursday they gave her another medicine and it looked like she was having a bad reaction to it....her eyes were open but she couldn't move her body. We were freaking out thinking something was wrong. I ended up crashing and had to be carried away. All the result of everything going on of course.Everyone on the staff was very frustrated at not being able to help her. We felt like we were loosing our baby.We continued slowly getting through the end of the week and weekend dealing with all the symptoms still. Dr came to the conclusion that he felt she had got a bad virus. Although, he never dismissed the fact that it could be the Singulair but said unfortunately there was no test to look for that. He said parents usually know their kids better than anyone though.Dr. said when she was released she would have to go to inpatient rehab because of the anxiety issues and because she had not walked for so long (4-5 weeks).Dr came in Monday morning and said if she did not start drinking more she was about 2 days away from a feeding tube. During the day she started drinking more and when he came back in that night he said she had drank enough and he took her off the IV and said she could go home and we could do outpatient rehab. We were so happy to take her home even though we knew it would be hard. So the next day, Tuesday, was very hard and we had very serious episodes with not talking, loss of hearing, shaking, still not walking and passing out. We called the Dr. at the hospital and they said it was all due to the anxiety. We were praying over her so hard. Well Wednesday she woke up and said she had no more pain, she was hungry, and she started walking again. We got our baby back! And there is no doubt in our mind that it was that Singulair. We know that it was. From the time we took her off of Singular to the time she was totally restored was 9 days. It happened just like the all the other parents had described. As soon as it was out of her system she all of a sudden came back to us. We decided to not take her back to those pediatricians. I recently took her for a follow up with her Allergist,who was not aware of what had happened and after hearing the story said that he had experienced two of his patients being allergic to Singulair and they had hallucinations. They were pulled off the medicine immediately so their cases were not as extreme as hers. Please be cautious! This was a devastating experience! Please feel free to email us. I have documented our whole story if you would like it emailed to you.

I have six year old twins who have been on Singulair since August. Things have been so bad I have considered putting them in counseling. The physical symptoms they have is dry, red eyes, stomach aches, stuffy nose, sore throat, cough, night sweats, body aches, itchy skin, cherry red cheeks and ears, and excessive weight gain. The other symptoms they suffer from are night terrors, sleep walking and reaching for things that are not there. Also anger, depression, very, very irritable they will cry over the least little things. They are doing well in school, but are crying every day they hate school and they basically hate everything. The teacher also tells me they can't pay attention. They have become very aggressive hitting each other and there brother and sister. Screaming and crying for long periods of time. I really started to worry when one of them said he wished he were dead. That is something a six year old should not even think of. I have four kids and I just thought it was family stress and it was because I couldn't devote enough attention to them. I had begun to think that I was the worst mother on the planet. With all these crazy things going on I never dreamed that they were connected. I really don't know why I goggled Singulair side effects, but I am so glad I did. It cannot be a coincidence that so many children and adults have the same symptoms and they all take Singulair. My children have taken their last dose tonight and I pray they will start feeling better. It is such a relief to know that there is a reason for their behavior it was so out of character for them. I usually do not reply to any posts but I feel it is important to let everyone know about this. I will also let my pediatrician know.

I am a 67 year old male. Very healthy other than high blood pressure and high cholesterol. I've been on BP drugs for 12 years or more and on Lipitor for aper 4 years or so. My cholesterol improved dramatically, but every joint in my body aches pretty badly until I start to move in the morning. (I am very active but do not engage in organized exercise...) As I think of it, these ache symptoms have increased steadily over the "Lipitor period".
I know most older folks endure some increase in aches and pains, but mine seem most extreme and are starting to affect my lifestyle.
Not much is written concerning my particular "Lipitor problem"......?????

hello everyone
i am a full time college student and I believe that i have some side effects from synthroid. As i was reading everyones blog i notice that some people feel the same way that i do. At times i feel that i'm normal but if something upsetting happens i get really tired, depress, and I have a never time concentrating at school and home. My body hurts all the time. especially my joints and i feel that i don't want to do anything. I have about a year left until i graduate and its the going to be hard. I cry sometimes for no reason. help! i'm going to talk to my doctor but if any body else feels the same way please reply.

Can someone tell me how long it took for the symptoms to go away.

I have been itchy, eye swelling, tingles, numbness in my hands and feet as well as a rash.

UPDATE FROM MORE4SURE :) .... i have been off Lisonopril now for one week, and i feel so much better i can hardly believe it! i occasionally get a little pain when i breath, and still an upset stomach alot but im hoping those issues will go away eventually. as for all the other problems i was experiencing during the 4 months i took Lisinopril, non stop coughing, constant headaches, blurred vision, shortness of breath, fever/chills/body aches etc, etc.. pretty much all gone. i no longer wake up every day tired, weak and unable to function normally. FEELING GREAT!! life is good again :) i hope my situation will help someone else who is having problems with this med. please feel free to email me ****** good luck and good health to all...

i have high BP and was on a med that worked well but was rather expensive, so i asked my Doc if we could try something more affordable. he put me on Lisinopril and within a few days of starting this med i had headaches, coughing, upset stomach and dizzyness. i assumed this would be temporary as per getting used to the new med, but it only got worse... and by 2 months later i was also having shortness of breath, constant fatigue and trouble sleeping. i looked up Lisinopril side effects online and called my Doc to say that i was having many problems with this med, he assured me it was not the Lisinopril and to keep taking it. on Sept 28th 2007, i went in to see the Doc and my BP was still a bit high so he doubled the dosage of Lisinopril. 2 days after i started the new dosage i had such serious breathing problems i was literally gasping for air and had to go to Emergicare, my BP had come down and the Doc at Emergicare said the breathing problems were just seasonal allergies and prescribed some Prednisone which he said would help. he also said i might want to come in for some Nebulizer treatments. i continued to take the double dosage of Lisinopril and was so sick every day that i no longer even cared what happened to me. i had a constant pounding headache, chills/body aches, blurred vision, nausea, weakness, coughing, fuzzy confused feeling, and i felt totally exhausted...breathing was still difficult and at night just rolling over in bed caused me to gasp for air. well 2 days ago i could not take it anymore and called my Doctors office to firmly explain that the med was making me VERY ill, they said they would get a message to my Doc right away and in like 5 minutes they called back and said STOP this med immediately!! well it's been 48 hours now since the last dose of Lisinopril and i feel much better already. i still have a headache but the other problems are fading down to very mild. i can even breath again YAY....i only hope that in a few more days i will feel normal again. to ANYONE reading this dont take this med, it will make you very, very sick!! and for those of you who actually are on this stuff please pay attention to how you are feeling and tell your Doctor right away, dont ignore the side effects.. make your Doctor listen and tell him how you feel even if it seems like mild issues bcause it will get worse!! good luck and peace to all.. :)

Ive been on Seroquel for quite some time now, I asked my doctor too get me off. I am also on Lithium and Welbutrin. I have lost 45 pounds. Which isnt a horrible thing but with out Seroquel I am awake all the time. I stay up for days. After day three i break down and take a Seroquel and wake up with the worse body aches ever. It feels like someone beat me up with a metal bat and put me back in bed. If I don't sleep for at least 11 hours I cannot get up and function much less do any daily activities.It also makes my depression worse, on top of my lithium. The bodyaches I cannot do any more.

I took one adult dosage of Bactrim for a small persistent skin rash on my ankle. That dose has leveled me in a few hours. Chest pains, trouble breathing, body aches, loss of appetite and nausea. I went to GNC to get calcium and folic acid since I read calcium folinate is used to treat adverse reactions. They have helped some, but I still feel pretty bad. I can kick myself for not researching Bactrim first as I would have never taken a single dose.

Russell

I've been on Synthroid for almost a year now, and I feel great. I was feeling so bad before, I had constant painful headaches, fatigue, nausea, dizziness, body aches it was horrible. Once I started the med I felt 100% better after a few days. However, if I miss a days dose or two I get my symptoms back full force.

I am a 19-year-old female pre-med student who has been taking this nasty drug for exacly 1 year now.... The amount I am on continues to change, for my disease keeps returning and leaving remission. I finally get down to 10mg from 40mg, and have to go back up when symptoms return!!! This is SO discouraging. The worst part is, no one understands the physical and emotional agony this drug brings on. I'm 19 and feel like I'm 90. My body aches, my weight is constantly fluctuating, I bruise from simply being poked (being a clumsy person, I look like I am beat!!), my bones feel as if they are about to break, and I am SEVERELY despressed. Being in college and taking rigorous classes, this is just too much for me to handle anymore... My 5-year relationship with the love of my life/best friend is falling apart because of my horrible mood swings.. don't blame him for leaving. I feel as if this drug has ruined my life more than the disease itself...Does ANYONE know if one's body and mind returns to "normal" after FINALLY being off this drug??? I pray to God the answer is yes... I would appreciate someone's reply and/or insight, because my Dr. fails to tell me about ANY side effects until I mention something. PLEASE REPLY!!!

took one dose of avelox at 830pm yesterday and then took one dose of hydrocodone for cough at 1100pm. Woke up 2 hours later with ankle & wrist joint pain, swollen flushed face and upper extremeities, completely bloodshot eyes(no visible whites), fever, chills, neck stiffness, itching on neck,shoulders and arms, general body aches, overall joint stiffness. saw doc today and he said conjunctivitis-prescribed drops, and that it was just the infection I had running it's course. Now my husband does not want me to take this evenings dose. perplexed as I have some underlying connective tissue disease and I am not sure if the joint stuff and redness is just due to being out in the sun yesterday without sunscreen and the aftermath

i encountered this site when i specifically searched for yasmin side effects. i could not believe it when i have read all the posts and how relieved i was to realize i wasn't dying or that i wasn't crazy. for the last 2 years i really wondered what was wrong with me, and i spent a fortune trying to find out to the extent that i underwent tumor marker tests last year for my thyroid. i was losing weight erratically, my migraine attacks were severe i literally became an invalid for a week. i haven't slept a goodnight's rest in 2 years, and only last week i thought i was sufferring a heart attack. all along i attributed it to stress at work, stress over my 2-year custody battle over my kids, and many other things. i did yoga, did a lot of meditation thinking i might be emotionally imbalanced. i wake up in the morning wanting to die, i wake up in the middle of the night with this god-awful feeling every time, and i thought that i might be one of those perenially depressed. i really took a good look about my life last week when i was down with severe migraine, nausea, body aches, heart palpitations, diarrhea and depression. what was causing this? nothing in my life, not with work, my kids are with me, i have a wonderful guy who puts through my moods and horrible temper, and a friend said the operative word, hormones. and bingo. this site came along. i came off yasmin 3 days ago after reading the posts. called my trusted doc from home and she confirmed this to be true. i am now sufferring heavy bleeding, i ache all over, and have teriible migraines. i read about withdrawal symptoms but not much. i hope i feel better soon. i wish that more doctors will know about this. and more women. this drug destroys lives.

I am 43 (female) and have been on Singulair for a couple of months now and the benefits have been AMAZING! I have chronic generalized eczema and pronounced facial flushing which led to swelling and Rosacea. Since starting Singulair (with a Zantac and Reactine) my skin is almost always cool (it's been YEARS). The benefits for me have been as great as what the steroids do for my skin. I can tolerate more triggers and the freedom and self-esteem boost is unquestionably life changing.

But recently I started to bruise, over every-little-thing -- even a blood pressure cup created a ring of broken blood vessels. Then about 3 - 4 weeks ago I started getting deep lower leg pain, and cramping in my calves and arches. This grew more regular, and my hips joined in and I am now rarely without the pain and deep aches. Then the weakness started, it was most pronounced in my dominant hand, I can hardly write or hold a pen now. Typing is difficult now as my hands and forearms are so weak. Yesterday I couldn't pinch my fingers to pick up a potatoe chip! My arches are curled with aches, I am weak all over and getting really uncoordinated. Going up the stairs is a chore, going down is just wacky -- it's harder than going up I am so wobbly and my knees want to give out. It's getting so pronounced that I realized that this must due to something I'm taking and the only thing I'm taking new is Singulair so I decided to Google "Singulair Side Effects" and the first link I clicked was Carrie's post, which I replied too. Then I realized there was more and have been reading all the other posts.

I am grateful that it is just side effects and nothing more sinister. This weekend the accumulated symptoms had me a bit frightened. I was washing my hands and it felt like I sprained my fingers doing it. The ligaments just sort of let go and things began bending the wrong way. It happened when I bent over to put something in the dishwasher, it was like the rib cage lost it's shape for a moment (I don't know how else to describe it). THAT felt bizarre and got my attention. Not being able to pinch my fingers to pick up a chip was the final clue that something is going wrong here. I will stop taking the Singulair now. It's a shame this happened, it was really doing it's job for me. The price of the side effects is too high though.

I was prescribed this for a UTI. I took ONE pill at 7 PM and by 8PM I was vomiting profusely and having diarrhea at the same time. I had a horrible headache and body aches, chills and probably a fever. Day two I feel exhausted and still have a horrible head ache. Unfortunately it is a holiday week end and I must wait to talk to the doctor until Tuesday about the UTI.

2 weeks ago I switched from Microgestion FE to Yasmin. I thought my slight pms would disappear with yasmin. What has followed has made my slight pms feel like a walk in the park.

5 days into the first week I had terrible nausea, heart palpitations and anxiety. A few days later started the body aches everywhere. i felt like i was actually dying. I found this website and went off the pill after 11 days, within 1 day I was so much better and almost totally better by 2-4 days.

A week later they gave me Yaz samples. Started those 4 days ago. I was vomiting this afternoon and now have seriously bad cramps in my hips and legs. i feel like i got hit by a truck. i have to assume its the pill, since it's so similar to the yasmin. what is strange is that i tried a pack or two of yaz a year ago with no problems that i recall. And although i am having the anxiety and mental side effects these physical ones are not something i am manifesting. I am not sure if my body has changed, or like another posted mentioned a reformulation. Never had side effects to bcps before either.

I have bipolar, and for a year I was willing to attribute my symptoms to that illness. I started the lisinopril when I moved and made a bunch of life changes, so I didn’t connect the onset of the symptoms with the med. Every night, though, I would get sick around 5 or 6 PM (I took lisinopril in the morning): nausea, headache, body aches, extreme lethargy, shortness of breath, fluttering feeling in my chest. These symptoms were so bad that twice I went to the emergency room. (Unfortunately, I presented as a bipolar patient with anxiety, so my treatment was less than comprehensive.) I swapped out all my bipolar meds to rule out drug interactions, but never touched lisinopril because I thought of it as a “safe drug”. My PCP (who prescribed the lisinopril) referred me to a cardiologist who did a battery of tests. I stopped the 30 day heart monitor after 3 weeks because every time I had cardiac symptoms, I checked out fine. The only option left seemed to be that the symptoms were psychosomatic, which scared me because I had no idea how to tackle that. I finally decided to investigate lisinopril and found this site by accident. It was amazing to read all the posts that were similar to my experiences. The day I discontinued the lisinopril in the morning, that night I did not get sick. I waited until I had been well for a week before concluding that the symptoms were indeed side effects of this med. It’s been a couple of months since I discontinued the lisinopril. And I have not been sick once, though I do struggle regularly with the bipolar. (I do monitor my blood pressure regularly: there’s a reason why everyone tells you to do that!) I feel stupid for not suspecting lisinopril earlier (I’m the kind of person who has a PDR and quizzes doctors on pharmacological modes of action) but I just thought that someone would flag it if there could be a problem.

I think those of us with a chronic illness tend to try to make symptoms fit within the framework of our known disease models. I’m writing a book and would welcome input on any aspect of bipolar or about dealing with chronic illness in general.

This site is a blessing. Congratulations on finding it!

Only now after the break up of my marriage and the begining of a new relationship,do i realise that something was just not right, when my new man was saying exactly the same things as my ex...terriable mood swings, constant angry feelings, scarring acne , constant tiredness and general body aches and pains, sore breasts, a slow but steady weight gain of nearly 4 stones inspite weight watchers etc and depression. Was on seroxat for a time until i saw a programme that highlighted side effects of that and so have lived with depression for years. A visit to ER with heart palputations which i thought was a heart attack. Panix attacks....I dont know why i suddenly thought that the mirena might have something to do with all this, thought i was going crazy , especially after my husband left me ...i had it removed last week and already feel better. Lost 4Lb in 5 days. Today i feel a little tired but still pleased its out. There is too much thats happened to me in the last 5 years for this to be a coincidence. My gp had no hesitation on removing it ....its too early to tell what will happen, but already i feel more peaceful...

I have been taking Synthroid for at least 10 years. I am on a very high dosage now175mcg. I have been on a lower dose but my counts were still low so my doctor put my dosage higher. I have been having a tremendous amount of body aches including finger joint aches and right flank problems. I have taken x-rays and various tests to determine what the pain is but I feel that after reading much of the side effects from this web site, much of what I am experiencing is from the Synthroid or Levothyroxin. I now feel that I need to take matters into my own hands and do more natural healing. Many doctors don't connect the dots to determine the real cause of your concerns.

Since changing from Synthroid to Levoxyl almost six months ago, I've gotten worse. I have much of the same symptoms as the one's i've read ie: headaches, swelling, numbness in fingers, fatigue, body aches, depression, hot and cold, but the latest one is very concerning for me, I never had allergies before, and now, my throat is always itchy, my ears are itchy, and it's making me crazy. Also, my fingers get numb and now at night my hands get very hot and itcy also. Can anyone out there relate? Thank you

I am really hoping someone can help me with the side effect issues I am having after taking Prednisone to cure a tumor on my larynx.. I was on the drug for six months.. taking 60 mg a day. It saved my life and at the same time it was just about to kill me, I am not kidding. The horrible effects it had on my body was really worse than the tumor that was taking my life. It would have almost been easy to die.
But today I'm very grateful for the miracle it did on my throat. I did not have a voice for many years.. today I can sing and that makes it's a great gift.
I was wondering, after being on it for so long and coming off nice and slowly, should my joints be in this much pain? My body aches are horrible.. all the muscles hurt and that never seems to go aways. Is this normal?

I am on my last shot and I am so Glad.I have had night sweats,hot flashes,sleeping diffuculties,no energy,achey and a little weightgain.I am curious to see how I feel once I am off this for good.If anyone has any ideas or any comments about Lupron let me know.

I am taking this for a bladder infection, and I have the worst body aches, and burning sensation in the bladder/vagina area. I feel tired, my stomach hurts, and not as alert as I should be, and I feel very negative.

I had a nose bleed which I rarely get, and just feel like garbage. The infection is getting better but I'm not so sure the side effects are worth it!

I had been taking Lipitor for several years and had many of the common problems listed as possible side effects, however, since bloodwork showed no liver problems my doctors kept me on the drug. In Novemeber 2005, I had a 'charlie-horse' so bad that it tore a muscle in my right leg.

I stopped taking the drug, but the damage was done! Since that time my condition has continued to go down hill and no doctor has been able to help.

I've been taking 50 mg. daily (and conscientiously) for several years. I've been taking thyroid supplements (synthroid and similar) for 35+ years. For 15 years, I've been struggling with the gradual weight gain commonly associated with menopause and stopping smoking cigarettes (after 30 years of 1+ packs daily). HOWEVER, It was about six years ago that the problem became a 50 lb. overweight and BMI in the waist-over-35" serious problem. I was always strong, quick to build muscle, and enjoyed being active. Swam .5 mi daily or walked 3 miles (or both) frequently until about menopause time. But then: about four years ago, I started having some pretty serious trouble breathing associated with exertion. Body aches and pains that I've described as arthritic, may also be involved here! Hence decreasing exercise and real worry about engaging in exercise. I've also been taking Lipitor and Avandia.
Frankly, I'm feeling that all my meds except Synthroid can cause me to gain weight - the catch 22 being that my elevated blood pressure and early type-2 diabetes are also negatively affected by overweight!! Now what???? Dr. appt, very soon, folks!